NDC Package 41163-158-60 Equaline Congestion Relief

Ibuprofen,Phenylephrine Hcl Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
41163-158-60
Package Description:
20 BLISTER PACK in 1 CARTON / 1 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Equaline Congestion Relief
Non-Proprietary Name:
Ibuprofen, Phenylephrine Hcl
Substance Name:
Ibuprofen; Phenylephrine Hydrochloride
Usage Information:
•do not take more than directed•adults and children 12 years of age and over:•take 1 tablet every 4 hours while symptoms persist.•do not use more than 6 tablets in any 24-hour period unless directed by a doctor•children under 12 years of age: do not use because this product contains too much medication for children under this age
11-Digit NDC Billing Format:
41163015860
NDC to RxNorm Crosswalk:
  • RxCUI: 1369775 - ibuprofen 200 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1369775 - ibuprofen 200 MG / phenylephrine hydrochloride 10 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    United Natural Foods, Inc. Dba Unfi
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA203200
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-17-2015
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 41163-158-60?

    The NDC Packaged Code 41163-158-60 is assigned to a package of 20 blister pack in 1 carton / 1 tablet, film coated in 1 blister pack of Equaline Congestion Relief, a human over the counter drug labeled by United Natural Foods, Inc. Dba Unfi. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 41163-158 included in the NDC Directory?

    Yes, Equaline Congestion Relief with product code 41163-158 is active and included in the NDC Directory. The product was first marketed by United Natural Foods, Inc. Dba Unfi on July 17, 2015 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 41163-158-60?

    The 11-digit format is 41163015860. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-241163-158-605-4-241163-0158-60